A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978818



Internal ID12979175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18625172..18780535hg38UCSC Ensembl
Innerchr13:19199312..19354675hg19UCSC Ensembl
Innerchr13:18097312..18252675hg18UCSC Ensembl
Innerchr13:18097312..18252675hg17UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38155364
hg19155364
hg18155364
hg17155364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34400
Supporting Variants
SamplesNA12716
Known GenesLINC00417
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978818
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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